Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:228457837-228458141 | Common:1; Rare:130 | ||||
chr1:229271027-229271307 | Rare:93 | ||||
chr1:229508209-229508445 | Common:1; Rare:95 | ||||
chr1:231241089-231241362 | Common:2; Rare:134; Clinvar:4; Clinvar (benign):2 | ||||
chr1:231337830-231338056 | Common:2; Rare:82 | ||||
chr1:231528506-231528758 | Common:2; Rare:86 | ||||
chr1:232950488-232950651 | Common:3; Rare:53 | ||||
chr1:233613862-233614179 | Common:5; Rare:93 | ||||
chr1:234373337-234373596 | Common:1; Rare:128; Clinvar (benign):4 | ||||
chr1:234373619-234373775 | Rare:63; Clinvar (benign):3 | ||||
chr1:235128782-235128964 | Rare:73 | ||||
chr1:235328151-235328627 | Common:4; Rare:147 | ||||
chr1:235866850-235867142 | Common:3; Rare:87 | ||||
chr1:236064972-236065333 | Common:3; Rare:131; Clinvar (pathogenic):1 | ||||
chr1:236523838-236524024 | Common:3; Rare:49 |